We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We are a global provider of co...
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As a Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.
You will have strong demonstrable experience in:
Designing, developing, validating and documenting SAS programs to generate analysis datasets, generate summary tables, figures and listings.
Support statisticians in the development and review of Statistical Analysis plans and programming specifications
Responsible for assisting data management with implementing protocols and CRFs
We are looking for:
Bachelors or Master's degree in statistics, biostatistics, or related field
SAS Programming experience – (ideally 3 yrs or more)
Major experience in the Pharmaceutical/CRO industry
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